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Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review

Heterotopic pancreas is a rare congenital abnormality that occurs during the growth and development process. It can be found in any part of the digestive tract, but the most common sites are the stomach, duodenum, and jejunum. Malignant transformation especially in the esophagus is rare. Here, we ai...

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Detalles Bibliográficos
Autores principales: Yang, Yong‐Bo, Liu, Yi‐Qiang, Dai, Liang, Yan, Wan‐Pu, Liang, Zhen, Chen, Ke‐Neng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977157/
https://www.ncbi.nlm.nih.gov/pubmed/35253375
http://dx.doi.org/10.1111/1759-7714.14344
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author Yang, Yong‐Bo
Liu, Yi‐Qiang
Dai, Liang
Yan, Wan‐Pu
Liang, Zhen
Chen, Ke‐Neng
author_facet Yang, Yong‐Bo
Liu, Yi‐Qiang
Dai, Liang
Yan, Wan‐Pu
Liang, Zhen
Chen, Ke‐Neng
author_sort Yang, Yong‐Bo
collection PubMed
description Heterotopic pancreas is a rare congenital abnormality that occurs during the growth and development process. It can be found in any part of the digestive tract, but the most common sites are the stomach, duodenum, and jejunum. Malignant transformation especially in the esophagus is rare. Here, we aim to report an unusual case of mid‐esophageal adenocarcinoma that originated from a heterotopic pancreas.
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spelling pubmed-89771572022-04-05 Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review Yang, Yong‐Bo Liu, Yi‐Qiang Dai, Liang Yan, Wan‐Pu Liang, Zhen Chen, Ke‐Neng Thorac Cancer Case Reports Heterotopic pancreas is a rare congenital abnormality that occurs during the growth and development process. It can be found in any part of the digestive tract, but the most common sites are the stomach, duodenum, and jejunum. Malignant transformation especially in the esophagus is rare. Here, we aim to report an unusual case of mid‐esophageal adenocarcinoma that originated from a heterotopic pancreas. John Wiley & Sons Australia, Ltd 2022-03-06 2022-04 /pmc/articles/PMC8977157/ /pubmed/35253375 http://dx.doi.org/10.1111/1759-7714.14344 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Yang, Yong‐Bo
Liu, Yi‐Qiang
Dai, Liang
Yan, Wan‐Pu
Liang, Zhen
Chen, Ke‐Neng
Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title_full Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title_fullStr Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title_full_unstemmed Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title_short Malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—A rare case report and comprehensive literature review
title_sort malignant transformation of heterotopic pancreas as middle esophagus adenocarcinoma—a rare case report and comprehensive literature review
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977157/
https://www.ncbi.nlm.nih.gov/pubmed/35253375
http://dx.doi.org/10.1111/1759-7714.14344
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